Phenotype #0000060847

Individual ID 00081270
Associated disease SLS
Phenotype details HP:0007503 (Generalized Ichthyosis); HP:0000989 (Pruritus); HP:0000982 (Palmoplantar keratoderma); HP:0001264 (Spastic diplegia, severe); Motor disability in arms (mild);
HP:0005656 (Positional foot deformity, moderate); HP:0001249 (intellectual disability, with mild speech disorder); HP:0000966 (Hypohidrosis); HP:0030507 (retinal crystals); HP:0000613 (photophobia)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 08y (8 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Maximilian Weustenfeld
Database submission license No license selected
Created by Maximilian Weustenfeld
Date created 2016-09-27 19:20:01 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.